JPH01196302A - Chemical treatment process for timber - Google Patents
Chemical treatment process for timberInfo
- Publication number
- JPH01196302A JPH01196302A JP2220588A JP2220588A JPH01196302A JP H01196302 A JPH01196302 A JP H01196302A JP 2220588 A JP2220588 A JP 2220588A JP 2220588 A JP2220588 A JP 2220588A JP H01196302 A JPH01196302 A JP H01196302A
- Authority
- JP
- Japan
- Prior art keywords
- water
- wood
- timber
- organic acid
- acid metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 15
- 239000000126 substance Substances 0.000 title claims description 3
- 229910052751 metal Inorganic materials 0.000 claims abstract description 28
- 239000002184 metal Substances 0.000 claims abstract description 28
- 150000003839 salts Chemical class 0.000 claims abstract description 24
- 150000007524 organic acids Chemical class 0.000 claims abstract description 20
- 150000001875 compounds Chemical class 0.000 claims abstract description 18
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 3
- 239000002023 wood Substances 0.000 claims description 65
- 239000007864 aqueous solution Substances 0.000 claims description 18
- -1 inorganic acid salt Chemical class 0.000 claims description 15
- 238000006116 polymerization reaction Methods 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 13
- 229920000642 polymer Polymers 0.000 abstract description 11
- 230000002265 prevention Effects 0.000 abstract description 2
- 230000000717 retained effect Effects 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 16
- 239000007788 liquid Substances 0.000 description 8
- 239000000077 insect repellent Substances 0.000 description 7
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000003063 flame retardant Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000011888 foil Substances 0.000 description 5
- 150000002484 inorganic compounds Chemical class 0.000 description 5
- 229910010272 inorganic material Inorganic materials 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- 229940048053 acrylate Drugs 0.000 description 4
- 238000005342 ion exchange Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 4
- CCHRVFZBKRIKIX-UHFFFAOYSA-N 1-nitro-3-(3-nitrophenyl)benzene Chemical class [O-][N+](=O)C1=CC=CC(C=2C=C(C=CC=2)[N+]([O-])=O)=C1 CCHRVFZBKRIKIX-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- LIQDVINWFSWENU-UHFFFAOYSA-K aluminum;prop-2-enoate Chemical compound [Al+3].[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C LIQDVINWFSWENU-UHFFFAOYSA-K 0.000 description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- XKMZOFXGLBYJLS-UHFFFAOYSA-L zinc;prop-2-enoate Chemical class [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C=C XKMZOFXGLBYJLS-UHFFFAOYSA-L 0.000 description 3
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical class CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 2
- 235000014466 Douglas bleu Nutrition 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 241000218683 Pseudotsuga Species 0.000 description 2
- 235000005386 Pseudotsuga menziesii var menziesii Nutrition 0.000 description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
- 241001673272 Tsuga diversifolia Species 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 238000007259 addition reaction Methods 0.000 description 2
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 2
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- TXTCTCUXLQYGLA-UHFFFAOYSA-L calcium;prop-2-enoate Chemical compound [Ca+2].[O-]C(=O)C=C.[O-]C(=O)C=C TXTCTCUXLQYGLA-UHFFFAOYSA-L 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- DWLAVVBOGOXHNH-UHFFFAOYSA-L magnesium;prop-2-enoate Chemical compound [Mg+2].[O-]C(=O)C=C.[O-]C(=O)C=C DWLAVVBOGOXHNH-UHFFFAOYSA-L 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 235000019837 monoammonium phosphate Nutrition 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229940047670 sodium acrylate Drugs 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 239000011592 zinc chloride Substances 0.000 description 2
- 235000005074 zinc chloride Nutrition 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical class COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- VAPQAGMSICPBKJ-UHFFFAOYSA-N 2-nitroacridine Chemical class C1=CC=CC2=CC3=CC([N+](=O)[O-])=CC=C3N=C21 VAPQAGMSICPBKJ-UHFFFAOYSA-N 0.000 description 1
- 235000007173 Abies balsamea Nutrition 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 241000218685 Tsuga Species 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 description 1
- 229910001626 barium chloride Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- CUXQLKLUPGTTKL-UHFFFAOYSA-M microcosmic salt Chemical compound [NH4+].[Na+].OP([O-])([O-])=O CUXQLKLUPGTTKL-UHFFFAOYSA-M 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、木材本来の化粧性や切削性を維持しつつ、木
質材に難燃性、態度、寸法安定性を付与する木材の化学
的処理方法に関するものである。[Detailed Description of the Invention] [Field of Industrial Application] The present invention is directed to the chemical treatment of wood that imparts flame retardancy, texture, and dimensional stability to wood while maintaining the natural cosmetic properties and cuttability of the wood. This relates to a processing method.
(従来の技術とその問題点〕
木材に硬度や耐摩耗性、寸法安定性等の物性を付与する
手段として、従来から木質材内の空隙部に樹脂やその他
の化合物を充填する所謂、樹脂注入法が広く知られてい
る。(Conventional technology and its problems) As a means of imparting physical properties such as hardness, abrasion resistance, and dimensional stability to wood, so-called resin injection has traditionally been used to fill voids in wood with resin or other compounds. The law is widely known.
この方法よれば、ポリエステルやアクリル等の合成樹脂
液の注入固化によって木材に硬度等の物性を付与するこ
とができるが、難燃性を付与することができない。According to this method, physical properties such as hardness can be imparted to wood by injecting and solidifying a synthetic resin liquid such as polyester or acrylic, but flame retardance cannot be imparted to the wood.
難燃性を付与するために、木材に水溶性の無機化合物を
含浸させることが知られているが、潮解したり溶出した
りして耐久性が損なわれることになる。It is known that wood is impregnated with water-soluble inorganic compounds in order to impart flame retardancy, but this results in deliquescence or elution, which impairs durability.
このため、特開昭61−246003号公報に開示され
ているように、混合することにより所望の不溶性不燃性
無機化合物を生じさせる2種の水溶性無機化合物を木材
中に順次含浸、混合させて不溶性不燃性無機化合物を分
散、定着させることが行われている。For this reason, as disclosed in Japanese Patent Application Laid-open No. 61-246003, two types of water-soluble inorganic compounds that produce a desired insoluble and nonflammable inorganic compound when mixed are sequentially impregnated into wood and mixed. Dispersion and fixation of insoluble, nonflammable inorganic compounds has been carried out.
しかしながら、この方法は、単に木材空隙内に上記処理
液の反応により析出した水不溶性の無機化合物を物理的
に充填させているだけであるために、微粉化して脱落し
たり表面が白化するという問題点がある。However, since this method simply physically fills the wood voids with water-insoluble inorganic compounds precipitated by the reaction of the above-mentioned treatment liquid, there are problems such as pulverization and falling off or whitening of the surface. There is a point.
又、処理液は汚染されるので、工業的に種々な工程を加
えなければならない。そこで、これを更に改良するため
に、難燃性樹脂類を含浸させて安定化する方法も検討さ
れているのが現状である。Furthermore, since the treatment liquid is contaminated, various industrial steps must be added. Therefore, in order to further improve this, a method of stabilizing it by impregnating it with flame-retardant resins is currently being considered.
本発明はこのような問題点に鑑みてなされたもので、木
質材に難燃性を付与する水可溶性ラジカル重合性有機酸
金属塩を含浸させて木質材内で木質材成分と金属塩とを
一体化させて水不溶性となし、木材の改質を図ることを
目的とするものである。The present invention was made in view of these problems, and involves impregnating wood with a water-soluble radically polymerizable organic acid metal salt that imparts flame retardancy, thereby combining the wood components and the metal salt within the wood. The purpose is to improve the quality of wood by making it water-insoluble by integrating it.
本発明者等は、上記目的を達成するために、種々研究を
行った結果、ラジカル重合性有機酸金属塩を必須成分と
する水可溶性ラジカル重合性化合物が水の存在下で木材
成分中の水酸基等の活性基と結合することに着目し、金
属架橋を持ったポリマーを木材中で生成させて木材と強
固に一体化させること、及び、ぎらには該ラジカル重合
性有機酸金属塩と水溶性無機酸塩類とがイオン交換反応
することに着目し、該不溶化した金属架橋ポリマーと水
溶性無機酸塩類を組み合わせて木材中に含浸させること
により、極めて優れた木材の改質効果が得られることを
見出して本発明に到達したものである。In order to achieve the above object, the present inventors have conducted various studies and found that a water-soluble radically polymerizable compound containing a radically polymerizable organic acid metal salt as an essential component is capable of forming hydroxyl groups in wood components in the presence of water. Focusing on bonding with active groups such as, we created a polymer with metal crosslinks in wood and firmly integrated it with the wood, and in addition, we created a polymer with metal crosslinks in the wood to firmly integrate it with the wood. Focusing on the ion exchange reaction between inorganic acid salts, we have found that by impregnating wood with a combination of the insolubilized metal crosslinked polymer and water-soluble inorganic acid salts, an extremely excellent wood modification effect can be obtained. This discovery led to the present invention.
即ち、本発明は、木質材に水可溶性のラジカル重合性有
機酸金属塩を必須成分とする水可溶性カシカル重合性化
合物水溶液を含浸させ、保水状態で重合反応させること
を特徴とする改質木材の製造方法、及び、木質材に水可
溶性のラジカル重合性有機酸金属塩を必須成分とする水
可溶性ラジカル重合性化合物水溶液を含浸させ、保水状
態で重合させた後、水溶性無機酸塩類を含浸させること
を特徴とする木材の化学的処理方法に係るものである。That is, the present invention provides a modified wood characterized by impregnating a wood material with an aqueous solution of a water-soluble radically polymerizable compound containing a water-soluble radically polymerizable organic acid metal salt as an essential component and causing a polymerization reaction in a water-retaining state. Production method, impregnating wood material with an aqueous solution of a water-soluble radically polymerizable compound containing a water-soluble radically polymerizable organic acid metal salt as an essential component, polymerizing it in a water-retaining state, and then impregnating it with a water-soluble inorganic acid salt. The present invention relates to a method for chemically treating wood, which is characterized by the following.
本発明方法において使用されるラジカル重合性有機酸金
属塩は、(メタ)アクリル酸の金属塩が最も一般的であ
り、中でも、アクリル酸ナトリウム、アクリル酸カリウ
ム、アクリル酸亜鉛、アクリル酸バリウム、アクリル酸
カルシウム、アクリル酸マグネシウム、アクリル酸アル
ミニウムなどの酸性塩は好都合に使用することができ、
特に、前記アクリル酸亜鉛、アクリル酸バリウム、アク
リル酸カルシウム、アクリル酸マグネシウム、アクリル
酸アルミニウム等の多価のラジカル重合性有機酸金属塩
は、重合するとそれ自体でも不溶化し、耐水性が良好で
ある。The most common radical polymerizable organic acid metal salts used in the method of the present invention are metal salts of (meth)acrylic acid, and among them, sodium acrylate, potassium acrylate, zinc acrylate, barium acrylate, acrylic acid, etc. Acid salts such as calcium acrylate, magnesium acrylate, aluminum acrylate can be advantageously used;
In particular, the polyvalent radically polymerizable organic acid metal salts such as zinc acrylate, barium acrylate, calcium acrylate, magnesium acrylate, and aluminum acrylate become insolubilized by themselves when polymerized, and have good water resistance. .
本発明の実施態様は種々あるが、通常はラジカル重合性
を機酸金属塩の水溶液を濃度20〜50%程度でpH2
〜6程度として調製する。Although there are various embodiments of the present invention, usually radical polymerizability is determined by preparing an aqueous solution of organic acid metal salt at a concentration of about 20 to 50% at pH 2.
Prepare to about 6.
又、上記ラジカル重合性有機酸金属塩の水溶液単独でも
よいが、さらに他の水可溶性のラジカル重合性化合物を
混入した水溶液は、−層強固な木質材との一体化が図ら
れ、改質効果が向上するので使用することがある。In addition, although an aqueous solution of the above-mentioned radically polymerizable organic acid metal salt may be used alone, an aqueous solution containing another water-soluble radically polymerizable compound can be integrated with the strong wood material and have a modification effect. It is sometimes used because it improves
このような水可溶性のラジカル重合性化合物としては、
グリセリンのジ(メタ)アクリレート、トリメチロール
プロパンジ(メタ)アクリレート、トリメチロールプロ
パントリアクリレート、ポリエチレングリコールモノ(
メタ)アクリレート、ポリエチレングリコールジ(メタ
)アクリレートなどの化合物が架橋剤の役割も果たして
使用することができる。Such water-soluble radically polymerizable compounds include:
Glycerin di(meth)acrylate, trimethylolpropane di(meth)acrylate, trimethylolpropane triacrylate, polyethylene glycol mono(
Compounds such as meth)acrylate and polyethylene glycol di(meth)acrylate can also be used as crosslinking agents.
上記水可溶性のラジカル重合性化合物をラジカル重合性
有機酸金属塩100部に対し、0〜10重量部の割合に
加える共に、これらの化合物の水溶液の重合開始剤とし
て過硫酸アンモニウム、過硫酸カリ、過酸化水素などの
水溶性過酸化物を使用して上記の化合物の総量に対し、
0.01〜5.0重量部を水溶液中に加える。The above-mentioned water-soluble radically polymerizable compound is added at a ratio of 0 to 10 parts by weight per 100 parts of the radically polymerizable organic acid metal salt, and ammonium persulfate, potassium persulfate, and persulfate are added as polymerization initiators for an aqueous solution of these compounds. For the total amount of the above compounds using water-soluble peroxides such as hydrogen oxide,
Add 0.01 to 5.0 parts by weight into the aqueous solution.
尚、上記重合開始剤は予め木材中に含有させておいても
よい。Incidentally, the above polymerization initiator may be contained in the wood in advance.
次いで、この水溶液を薄板、小片、ブロック等の木材に
常圧、又は、減圧、加圧等の組み合わせによって含浸さ
せる。Next, this aqueous solution is impregnated into wood such as thin plates, small pieces, blocks, etc. under normal pressure or a combination of reduced pressure, increased pressure, etc.
この場合、木材がブロックのように肉厚形状のものであ
れば、その表層部のみに難燃性を付与する目的で常圧下
での浸漬処理のような表面処理方法を採用してもよい。In this case, if the wood is thick-walled like a block, a surface treatment method such as immersion treatment under normal pressure may be employed in order to impart flame retardancy only to the surface layer.
上記水溶液を木質材に含浸後、直ちに、又は放置養生し
た後、できる限り水分が飛散しない状態で加熱重合する
。Immediately after impregnating the wood material with the above aqueous solution, or after being left to cure, heating and polymerization is carried out in a state in which water is not scattered as much as possible.
具体的には、木質材をアルミ箔やポリエチレン、ポリエ
ステルフィルム等で被覆し、オーブン加熱やオートクレ
ーブ加熱するか、又はホットプレスで両面加熱する。又
、オートクレーブ中で蒸煮により加熱してもよい。Specifically, a wooden material is covered with aluminum foil, polyethylene, polyester film, etc., and heated in an oven or autoclave, or heated on both sides with a hot press. Alternatively, it may be heated by steaming in an autoclave.
この際、加熱温度は保有水分によりバンクが生じないで
重合反応が進行するゆるやかな条件とすることが望まし
く、60〜150°C1好ましくは80〜110°C程
度である。At this time, the heating temperature is desirably a gentle condition in which the polymerization reaction proceeds without forming banks due to retained moisture, and is preferably about 60 to 150°C, preferably about 80 to 110°C.
このように保水状態で重合反応を生じさせるのは、木材
成分中の水酸基等の活性基とラジカル重合性有機酸金属
塩とが付加反応することにより木材成分の側鎖に高分子
化合物を修飾させることができることに着目したからで
ある。In this way, the polymerization reaction occurs in a water-retaining state by modifying the side chains of the wood component with a polymer compound through an addition reaction between active groups such as hydroxyl groups in the wood component and a radically polymerizable organic acid metal salt. This is because we focused on what is possible.
こうして保水状態での重合反応後、引き続いて又は別途
に適当な含水率まで木質材を乾燥させる。After the polymerization reaction in a water-retaining state, the wood material is subsequently or separately dried to an appropriate moisture content.
以上の方法が本発明における第1番目に記載した改質木
材の製造方法であり、処理液が水溶液であるから、木質
材を膨潤させながら木質材内の微小空隙まで浸透すると
共に水の存在下でラジカル重合性有機酸金属塩と木材成
分中の活性基とが付加反応するために、木材成分に高分
子化合物が修飾されると同時に木材空隙中に充填されて
水不溶性の有機酸金属塩ポリマーが木質材に含有される
ことになり、難燃性が付与されるものである。The above method is the first method for producing modified wood according to the present invention, and since the treatment liquid is an aqueous solution, it penetrates into the minute voids in the wood while swelling the wood, and in the presence of water. As a result of the addition reaction between the radically polymerizable organic acid metal salt and the active group in the wood component, the wood component is modified with the polymer compound and at the same time, the wood pores are filled into the water-insoluble organic acid metal salt polymer. is contained in the wood material, imparting flame retardancy.
特に、多価金属の有機酸塩ポリマーは架橋された形とな
り、水不溶の高分子を形成すると共に木質材を修飾して
いるので、木質材と強固に一体化して木質材の通常の使
用状態では上記高分子が溶出することがなく、難燃性等
の性能が長期間維持される。又、このように改質された
木材は、湿度を保持する効果もあり、寸法安定化が図れ
ると共に割れ防止作用も奏するものである。In particular, organic acid salt polymers of polyvalent metals are cross-linked, forming water-insoluble polymers and modifying wood materials, so they are strongly integrated with wood materials and can be used under normal conditions. In this case, the above-mentioned polymer does not elute, and performance such as flame retardancy is maintained for a long period of time. In addition, the wood modified in this manner has the effect of retaining humidity, is dimensionally stable, and has the effect of preventing cracking.
次に、本発明における第2番目に記載の方法について説
明すると、この方法は、第1番目に記載の方法によって
得られる改質木材の耐久性や難燃性を更に向上させると
共に防腐、防虫性を木質材に付与するためになされたも
のである。Next, the second method of the present invention will be explained. This method further improves the durability and flame retardancy of the modified wood obtained by the first method, and also has antiseptic and insect repellent properties. This was done to impart this to wood materials.
即ち、第1番目の発明において、木質材に処理液を含浸
させて保水状態で重合させた後、引き続いて、又は木質
材を適当な含水率に調整した後、この木質材に水溶性無
機酸塩類を含浸させてイオン交換反応を行わせることに
より上記水溶性無機酸塩も不溶化し、固定することを特
徴とするものである。That is, in the first invention, after a wood material is impregnated with a treatment liquid and polymerized in a water-retaining state, the wood material is subsequently impregnated with a water-soluble inorganic acid or after the wood material is adjusted to an appropriate moisture content. The water-soluble inorganic acid salt is also insolubilized and fixed by impregnating it with salt and performing an ion exchange reaction.
上記水溶性の無機酸塩類としては、塩化カルシウム、リ
ン酸ナトリウム、リン酸水素二ナトリウム、リン酸二水
素ナトリウム、リン酸水素二アンモニウム、リン酸二水
素アンモニウム、リン酸水素アンモニウムナトリウム、
硫酸アルミニウム、硫酸亜鉛、ケイ酸ナトリウム、ケイ
酸カリウム、塩化マグネシウム、塩化バリウム、塩化亜
鉛、ホウ酸ナトリウムなどがあり、難燃性の他にも防虫
防腐性、硬度、外観等の種々の目的に応じて単独又は二
種以上混合して使用できる。The water-soluble inorganic acid salts include calcium chloride, sodium phosphate, disodium hydrogen phosphate, sodium dihydrogen phosphate, diammonium hydrogen phosphate, ammonium dihydrogen phosphate, sodium ammonium hydrogen phosphate,
Aluminum sulfate, zinc sulfate, sodium silicate, potassium silicate, magnesium chloride, barium chloride, zinc chloride, sodium borate, etc. are used for various purposes such as flame retardant, insect repellent, hardness, and appearance. Depending on the situation, they can be used alone or in combination.
このような水溶性無機酸塩類を上記木質材に含浸させる
と、木質材中のラジカル重合性有機酸金属塩ポリマーと
この水溶性無機酸塩類とがイオン交換反応などを行って
金属架橋をもったポリマーと無機酸塩類が木材中に不溶
化して定着し、木質材の難燃性を向上させるばかりでな
く、耐久性を大幅に向上させることができるものである
。When such water-soluble inorganic acid salts are impregnated into the wood material, the radically polymerizable organic acid metal salt polymer in the wood material and the water-soluble inorganic acid salts undergo an ion exchange reaction to form metal crosslinks. The polymer and inorganic acid salts are insolubilized and fixed in the wood, which not only improves the flame retardance of the wood but also significantly improves its durability.
次に、本発明の実施例を示す。Next, examples of the present invention will be shown.
〔実施例1]
pH2のアクリル酸アルミニウム30%の水溶液に0.
3%の過硫酸アンモニウムを加えて含浸液とした。この
含浸液を厚さ2nuwのへイツガ単板に30T0■の減
圧下で含浸し、この含浸処理単板をアルミ箔にて被覆し
て24時間放置後、105°Cで3時間重合反応を行い
、その後、同じ温度で2時間乾燥した。[Example 1] 0.0% to a 30% aqueous solution of aluminum acrylate at pH 2.
3% ammonium persulfate was added to prepare an impregnating solution. This impregnating solution was impregnated into a 2nuw thick Hetsuga veneer under a reduced pressure of 30T0■, and the impregnated veneer was covered with aluminum foil and left for 24 hours, followed by a polymerization reaction at 105°C for 3 hours. , and then dried at the same temperature for 2 hours.
こうして得られた処理単板は極めて硬く、重量増加率は
43%で、防虫性、難燃性を有し、自然なベイツガの外
観を備えていた。The treated veneer thus obtained was extremely hard, had a weight increase rate of 43%, was insect repellent, flame retardant, and had a natural hemlock appearance.
〔実施例2]
pH5のアクリル酸亜鉛30%水溶液に30%過酸化水
素水2%を加えたものを含浸液として、3mm厚さのベ
イマツ単板に30T0RRの減圧下で含浸し、この含浸
処理単板をアルミ箔にて被覆し、24時間放置後、10
5°Cで3時間重合反応を行い、その後、同じ温度で2
時間乾燥した。[Example 2] A 3 mm thick Douglas fir veneer was impregnated with a 30% aqueous solution of zinc acrylate at pH 5 and 2% of a 30% hydrogen peroxide solution under a reduced pressure of 30T0RR, and this impregnation treatment was carried out. Cover the veneer with aluminum foil, leave it for 24 hours, and then
The polymerization reaction was carried out at 5°C for 3 hours, and then at the same temperature for 2 hours.
Dry for an hour.
こうして得られた処理単板は極めて硬く、重量増加率は
43%で、防虫性、難燃性を有し、ベイマツの自然な外
観を備えていた。The treated veneer thus obtained was extremely hard, had a weight increase rate of 43%, was insect repellent, flame retardant, and had the natural appearance of Douglas fir.
[実施例3〕
pH6のアクリル酸ナトリウム50%水溶液に2%のト
リメチロールプロパントリアクリレートを溶解し、更に
重合開始剤として0.5%の過硫酸アンモニウムを溶解
したものを含浸液とし、この含浸液を厚さ2■のベイツ
ガ単板に3QTOIIKの減圧下で含浸した。この含浸
処理単板をアルミ箔で被覆し、常温で24時間放置後、
105°Cで3時間重合反応し、引き続き塩化亜鉛20
%、ホろ砂3%の水溶液に浸漬し、再度、30TolK
における該水溶液の減圧含浸と24時間の熟成を行った
のち水洗し、105 ’C12時間の乾燥を行ったとこ
ろ、防虫性を有する硬質で難燃性の処理単板を得た。[Example 3] An impregnation solution was prepared by dissolving 2% trimethylolpropane triacrylate in a 50% aqueous solution of sodium acrylate at pH 6, and further dissolving 0.5% ammonium persulfate as a polymerization initiator. was impregnated into a 2-inch-thick Japanese hemlock veneer under reduced pressure using 3QTOIIK. After covering this impregnated veneer with aluminum foil and leaving it at room temperature for 24 hours,
Polymerization reaction was carried out at 105°C for 3 hours, and then zinc chloride 20
%, borax was soaked in a 3% aqueous solution of 30 TolK again.
After being impregnated with the aqueous solution under reduced pressure and aging for 24 hours, the veneer was washed with water and dried for 12 hours at 105'C to obtain a hard flame-retardant treated veneer with insect repellent properties.
〔実施例4〕
pH5,5のアクリル酸バリウム50%水溶液に5%過
酸化水素水1%(対重合性塩)を加えたものを含浸液と
して、この含浸液を11厚さのベイツガ単板に30T0
11Rの減圧下で含浸液を含浸させたのち、この単板を
アルミ箔にて被覆し、24時間放置後、105°Cで3
時間重合反応を行い、その後、同じ温度でアルミ被覆を
除いて2時間乾燥した。[Example 4] A 50% aqueous solution of barium acrylate with a pH of 5.5 and 1% of a 5% hydrogen peroxide solution (anti-polymerizable salt) was used as an impregnating liquid, and this impregnating liquid was used to coat a 11-thick Japanese hemlock veneer. to 30T0
After impregnating the veneer with the impregnating liquid under a reduced pressure of 11R, the veneer was covered with aluminum foil, left for 24 hours, and then heated at 105°C for 3 hours.
The polymerization reaction was carried out for a period of time, and then the aluminum coating was removed and dried at the same temperature for 2 hours.
こうして得られた処理単板は木目の白線模様が美麗であ
り、しかも、極めて硬く、重量増加率は85%で、防−
土性、難燃性を有し、床材として優れたものであった。The treated veneer thus obtained has a beautiful white line pattern in the wood grain, is extremely hard, has a weight increase rate of 85%, and is resistant to corrosion.
It has earthy properties and flame retardancy, making it an excellent flooring material.
〔実施例5〕
上記実施例4で得た処理単板を飽和リン酸二水素アンモ
ニウム水溶液に含浸し、24時間放置後、さらに乾燥し
た。[Example 5] The treated veneer obtained in Example 4 above was impregnated with a saturated aqueous ammonium dihydrogen phosphate solution, allowed to stand for 24 hours, and then further dried.
こうして得られた処理単板は、重量増加率は95%で、
防虫性、難燃性を有し、木目の白色模様はさらに美敷く
強調されていた。又、この単板を蒸留水に24時間浸漬
して乾燥後の減量を調べたところ、約2%であり、含浸
剤は安定化されていた。The treated veneer thus obtained had a weight increase rate of 95%,
It has insect repellent and flame retardant properties, and the white pattern of the wood grain is even more beautiful and emphasized. Further, when this veneer was immersed in distilled water for 24 hours and the weight loss after drying was examined, it was approximately 2%, indicating that the impregnating agent was stabilized.
以上のように本発明の木材の化学的処理方法によれば、
水溶性ラジカル重合性有機酸金属塩などの化合物が水の
存在下で木材成分中の水酸基等の活性基と結合して金属
架橋を持ったポリマーを木材中で生成し、木材と強固に
一体化して木材に長期間に亘る難燃性を付与することが
できると共に寸法安定性、硬度、割れ防止等の向上を図
ることができるものであり、さらに、上記ラジカル重合
性を機酸金属塩と水溶性無機酸塩類とをイオン交換反応
などさせることによって水溶性無機酸塩を不溶化し、そ
の状態で固定することにより木材の耐久性や難燃性を更
に向上させることができると共に防腐、防虫性等を木材
に付与することができるものである。As described above, according to the method for chemically treating wood of the present invention,
Compounds such as water-soluble radically polymerizable organic acid metal salts combine with active groups such as hydroxyl groups in wood components in the presence of water to produce polymers with metal crosslinks in the wood, which firmly integrate with the wood. It can impart long-term flame retardancy to wood and improve dimensional stability, hardness, crack prevention, etc. Furthermore, the radical polymerizability can be improved by combining organic acid metal salts and water-soluble Water-soluble inorganic acid salts are made insolubilized through an ion exchange reaction with water-soluble inorganic acid salts, and by fixing them in that state, the durability and flame retardance of wood can be further improved, as well as antiseptic and insect repellent properties. can be applied to wood.
Claims (2)
塩を必須成分とする水可溶性ラジカル重合性化合物水溶
液を含浸させ、保水状態で重合反応させることを特徴と
する木材の化学的処理方法。(1) A method for chemically treating wood, which comprises impregnating wood with an aqueous solution of a water-soluble radically polymerizable compound containing a water-soluble radically polymerizable organic acid metal salt as an essential component, and causing a polymerization reaction in a water-retaining state. .
塩を必須成分とする水可溶性ラジカル重合性化合物水溶
液を含浸させ、保水状態で重合させた後、水溶性無機酸
塩類を含浸させることを特徴とする木材の化学的処理方
法。(2) Impregnating wood with an aqueous solution of a water-soluble radically polymerizable compound containing a water-soluble radically polymerizable organic acid metal salt as an essential component, polymerizing it in a water-retaining state, and then impregnating it with a water-soluble inorganic acid salt. A chemical treatment method for wood characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2220588A JPH0681681B2 (en) | 1988-02-01 | 1988-02-01 | Chemical treatment of wood |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2220588A JPH0681681B2 (en) | 1988-02-01 | 1988-02-01 | Chemical treatment of wood |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01196302A true JPH01196302A (en) | 1989-08-08 |
JPH0681681B2 JPH0681681B2 (en) | 1994-10-19 |
Family
ID=12076290
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2220588A Expired - Lifetime JPH0681681B2 (en) | 1988-02-01 | 1988-02-01 | Chemical treatment of wood |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0681681B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03169504A (en) * | 1989-11-30 | 1991-07-23 | Miroku Kihan Kk | Modified woody material and modifying method for woody material |
US5605767A (en) * | 1993-06-09 | 1997-02-25 | Triangle Pacific Corporation | Hardened and fire retardant wood products |
US5731096A (en) * | 1995-08-04 | 1998-03-24 | Hydro-Quebec | Permanent decrease of wood hardness by in situ polymerization of pre-polymers |
WO2001087560A1 (en) * | 2000-05-15 | 2001-11-22 | HYDRO-QUéBEC | Permanent decrease of wood hardness |
JP2009166280A (en) * | 2008-01-11 | 2009-07-30 | Miro Mocle Sangyo Kk | Manufacturing method of reformed woody material, and reformed woody material |
JP2016102095A (en) * | 2014-11-28 | 2016-06-02 | 四国建設株式会社 | Wood preservative, method of producing processed wood using the same, and processed wood |
CN116214654A (en) * | 2023-02-08 | 2023-06-06 | 千年舟新材科技集团股份有限公司 | Fast-growing wood reinforcing process |
-
1988
- 1988-02-01 JP JP2220588A patent/JPH0681681B2/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03169504A (en) * | 1989-11-30 | 1991-07-23 | Miroku Kihan Kk | Modified woody material and modifying method for woody material |
US5605767A (en) * | 1993-06-09 | 1997-02-25 | Triangle Pacific Corporation | Hardened and fire retardant wood products |
US5609915A (en) * | 1993-06-09 | 1997-03-11 | Triangle Pacific Corporation | Hardened and fire retardant wood products |
US5683820A (en) * | 1993-06-09 | 1997-11-04 | Triangle Pacific Corporation | Hardened and fire retardant products |
US5731096A (en) * | 1995-08-04 | 1998-03-24 | Hydro-Quebec | Permanent decrease of wood hardness by in situ polymerization of pre-polymers |
WO2001087560A1 (en) * | 2000-05-15 | 2001-11-22 | HYDRO-QUéBEC | Permanent decrease of wood hardness |
JP2009166280A (en) * | 2008-01-11 | 2009-07-30 | Miro Mocle Sangyo Kk | Manufacturing method of reformed woody material, and reformed woody material |
JP2016102095A (en) * | 2014-11-28 | 2016-06-02 | 四国建設株式会社 | Wood preservative, method of producing processed wood using the same, and processed wood |
CN116214654A (en) * | 2023-02-08 | 2023-06-06 | 千年舟新材科技集团股份有限公司 | Fast-growing wood reinforcing process |
CN116214654B (en) * | 2023-02-08 | 2024-03-29 | 千年舟新材科技集团股份有限公司 | Fast-growing wood reinforcing process |
Also Published As
Publication number | Publication date |
---|---|
JPH0681681B2 (en) | 1994-10-19 |
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